FDA Inspection 974283 — Topcon Corporation

Topcon Corporation — FEI 1000175127

The FDA completed an inspection of Topcon Corporation on Mar 16, 2016 in Itabashi. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 16, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Itabashi (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.